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Published on: June 30, 2011
Endoplasmic reticulum-mediated phagocytosis is a mechanism of entry into macrophages
Etienne Gagnon1, Sophie Duclos, Christiane Rondeau
1Département de Pathologie et Biologie Cellulaire, Université de Montréal, Montréal, Québec, Canada.
Abstract:
Phagocytosis is a key aspect of our innate ability to fight infectious diseases. In this study, we have found that fusion of the endoplasmic reticulum (ER) with the macrophage plasmalemma, underneath phagocytic cups, is a source of membrane for phagosome formation in macrophages. Successive waves of ER become associated with maturing phagosomes during phagolysosome biogenesis. Thus, the ER appears to possess unexpectedly pluripotent fusion properties. ER-mediated phagocytosis is regulated in part by phosphatidylinositol 3-kinase and used for the internalization of inert particles and intracellular pathogens, regardless of their final trafficking in the host. In neutrophils, where pathogens are rapidly killed, the ER is not used as a major source of membrane for phagocytosis. We propose that intracellular pathogens have evolved to adapt and exploit ER-mediated phagocytosis to avoid destruction in host cells.
Insights
The endoplasmic reticulum (ER) provides membrane for phagosome formation in macrophages, a process vital for fighting infections. This ER-mediated phagocytosis is exploited by pathogens to evade destruction.
Area of Science:
- Cell Biology
- Immunology
- Infectious Diseases
Background:
- Phagocytosis is a critical innate immune mechanism for pathogen clearance.
- The source of membrane for phagosome formation in macrophages has been a subject of investigation.
Purpose of the Study:
- To investigate the role of the endoplasmic reticulum (ER) in phagosome formation.
- To understand the mechanisms and implications of ER involvement in phagocytosis.
Main Methods:
- Studied membrane dynamics during phagocytosis in macrophages.
- Investigated the involvement of phosphatidylinositol 3-kinase in ER-mediated phagocytosis.
Main Results:
- Identified fusion of the ER with the macrophage plasma membrane as a primary source of phagosome membrane.
- Observed successive ER association with maturing phagosomes during phagolysosome biogenesis.
- Found ER-mediated phagocytosis is regulated by phosphatidylinositol 3-kinase and utilized for various cargo, unlike in neutrophils.
Conclusions:
- The endoplasmic reticulum exhibits versatile fusion capabilities, contributing significantly to phagocytosis in macrophages.
- Intracellular pathogens may exploit ER-mediated phagocytosis for survival and evasion of host defenses.
- ER involvement in phagocytosis appears to be cell-type specific, differing between macrophages and neutrophils.
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